Title: Transport/Circulatory System
1Transport/Circulatory System
- Blood
- Heart
- Circulation
- Lymphatics
- Immunity
2Human Circulatory System
- Blood
- Heart
- Arteries
- Arterioles
- Capillaries
- Venules
- Veins
- Lymph Vessels
- Lymph Fluid
3Functions of Blood
- 3 Major Functions of Blood are
- Transport
- Regulation
- Protection
4Blood Composition
- Blood consists of 2 main parts
- Plasma (55)
- Cells (Red Blood Cells, White Blood Cells,
Platelets) (45)
5Blood Composition
- Plasma (55)
- Amber coloured fluid (92)
- Dissolved materials (8)
- Nutrients (sugars, amino acids, vitamins)
- Gases (O2 CO2)
- Hormones (Chemical Messengers)
- Antibodies (infection fighters)
- Proteins (eg. Prothrombin)
- Salts (Sodium Chloride, Bicarbonate)
- Wastes (eg. Urea, Heat)
6Blood Composition
- 2. Cells (45)
- Red Blood Cells
- Red blood cells (RBC) make up most of the
cellular part of blood. - White Blood Cells
- defenders of the blood circulatory system.
- Platelets
- involved in clotting (initiate clotting process)
7RBCs
- Red Blood Cells
- aka. Erythrocytes (erythro meaning red in
Greek) - Physical Appearance
- Small ( 8 ?m in diameter)
- Biconcave Disks
8RBCs
- No Nucleus
- Very Numerous
- 3 4 month lifespan
- Dead RBCs broken down by liver
- New RBCs are produced by bone marrow
- Contains hemoglobin (iron rich pigment)
9RBCs
- Function
- Carry O2 and CO2
- O2 Hemoglobin Oxyhemoglobin
- CO2 Hemoglobin Carbaminohemoglobin
- Hemoglobin will also carry Carbon monoxide
10RBCs
- Disorder Anemia
- Not enough RBCs in the blood
- Symptoms
- Fatigue
- Listlessness
- Increased susceptibility to other diseases
- Treatment
- Rest
- Increased Iron intake
11RBCs
- Sickle Cell Anemia
- Caused by a Mutant Gene producing defective
hemoglobin - Results in RBCs curving like a sickle
- Symptoms of anemia due to defective hemoglobin
and not enough oxygen being carried to the cells
12Sickle Cell Anemia
- Abnormal cells tend to form clumps and clog
smaller blood vessels causing decrease in
circulation - Severe pain in abdomen, back, head, and
extremities - Enlargement of heart, atrophy in brain cells
- Cells die (hemolyze) easily resulting in severe
anemia - Victims tend to suffer early death
- Evolutionary Benefits
- People who have heterozygous state suffer only
slight symptoms, but have a resistance to malaria
13WBCs
- White Blood Cells
- aka. Leukocytes
- Function
- Defend the body against foreign invaders
14WBCs
- Have a Nucleus
- 1 WBC to every 600 RBCs
- Physical Appearance
- larger than RBCs (10 µm)
- generally round, but can change shape
15WBCs
- Disorder Leukemia
- Cancer of blood forming organs
- Increase in WBCs
- Decrease in RBCs, results in Anemia
- Immense number of WBCs do not mature
- Treatment
- Cancer Treatments
- Bone marrow transplant
16WBCs
White Blood Cells White Blood Cells
Granular WBCs (Granulocytes) Non-granular WBCs (Agranulocytes)
Neutrophils Eosinophils Basophils Lymphocytes Monocytes
17WBCs
- Granulocytes
- Formed in bone marrow
- granules in the cytoplasm
- Irregular-shaped nuclei
- Short-lived
-
18WBCs
- Neutrophils
- 65 of WBCs
- actively phagocytic
- engulfs foreign invaders
19WBCs
- Eosinophils
- 2-4 of WBCs
- Destroy foreign proteins
- Break up blood clots
20WBCs
- Basophils
- 0.5 of WBCs
- Contains Histamine
- Initiates swelling
- Contains Heparin
- Anticoagulant
21WBCs
- Lymphocytes
- Makes up 20-25 of WBCs
- Two types
- B-Cells
- Forms antibodies
- T-Cells
- Memory Storage
22WBCs
- Monocytes
- 3-8 of WBCs
- Actively phagocytic
- Macrophages - can eat up to 100 bacteria at a time
23Platelets
- Platelets
- Smaller than RBCs
- 3 µm in diameter
- Contains
- Thromboplastin
- Serotonin
24Platelets
- Disorder Hemophilia
- Affects mostly males
- Inability to form blood clots
- Cause
- Genetic
- Mutant gene codes for defective protein
- Treatment
- Injections of missing protein
25Blood Clotting Cascade
- If a blood vessel is damaged
- Platelets are fragile cells, when they hit a part
of damaged wall (torn vessel), they break open. - Serotonin (hormone) is released, causing
vasoconstriction - Thromboplastin (protein) is released, activating
prothrombin (plasma protein). - Prothrombin ? Thrombin
26Blood Clotting Cascade
- Thrombin reacts with fibrinogen causing the
formation of fibrin (fibers) - Fibrin mesh traps RBCs
- Mesh RBCs Blood Clot (Thrombus)
27Clotting Cascade Review
Thromboplastin Calcium Prothrombin
Thrombin Fibrinogen
Fibrin (clot) Fibrin (clot) Fibrin (clot) Fibrin (clot) Fibrin (clot)
28Dangers of Blood Clotting
- Blood clots prevent the passage of blood
- Area tissues do not get oxygen
- If occurs in brain ? stroke
- If occurs in heart vessel ? may have heart attack
- A dislodged clot in vessel embolus
- May get caught in a vessel in a vital organ,
causes embolism (coronary, pulmonary)
29Blood - Whats Your Type?
- Historically, sometimes blood transfusions would
keep people alive, other times it wouldnt. Why? - Karl Landsteiner found that different blood types
existed. - Glycoproteins on RBCs determine blood type
- Type A, B, AB, or O
- Glycoproteins (A or B) are called antigens
- Type O has no glycoproteins
- Type AB has both A and B
30Blood - Frequencies
O A B AB
NA White 45 41 10 4
NA Black 47 28 20 5
Peruvian Indian 100
31Blood Antigen-Antibody Response
- How does the body recognize blood type?
- Body has antibodies for the other antigen (e.g.
Type A person will have Anti-B antibodies) - Antibodies respond to invaders by binding to
surface proteins - With blood, RBC of a different type will
agglutinate, or clump.
32Blood Antigen-Antibody Response
Blood Type Blood Contains Blood Contains
Cellular Antigens Plasma Antibodies
O None Anti A Anti B
A A Anti B
B B Anti - A
AB AB None
33Blood - To whom can I donate?
- Successful transfusion can occur provided the
plasma of the patient and the erythrocytes of the
donor are compatible. - For example
- Kevin (Type A) can donate to Michelle (Type A)
and Donnie (Type AB)
34Blood - To whom can I donate?
- A person with what blood type would be considered
a Universal Donor? - Type O
- Why?
- A person with what blood type would be considered
a Universal Recipient? - Type AB
35Rhesus Factor The Monkey Factor
- A different blood antigen
- Genetically determined
- Two types Rh- and Rh
- 83.3 of population are Rh (protein present)
- 16.6 of population are Rh (protein absent)
- Rh- will develop the Rh antibody only when
exposed to Rh blood - Blood donating Rh can receive from Rh-, but Rh-
cannot receive from Rh
36Rhesus Factor The Monkey Factor
- Important for pregnant women
- If there is a tear in the placenta, babies and
moms blood cells can enter each others blood
stream - If mother is Rh- and baby is Rh, the babies RBC
will stimulate the production of Rh antibodies by
the mother - Erythroblastosis fetalis If the mothers Rh
antibodies enter the babies blood stream, they
will cause agglutination and destruction of
babies RBCs, resulting in death of the baby. - Treatment
- Immunization of the mother with Rhogam or
Wingam- medicines that prevent the formation of
Rh antibodies (contain Rh anti-antibodies)
37Next The Circulatory System